Structure Information
Structure

Compound Identification

SMILES

CN(C)C1C(CO)OC(C1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=CNRXXRJDMFDIEY-UHFFFAOYSA-N

Formula

C12H18N6O3

Mass

294.315

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 3'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 3'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 3'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Pyrimidine - N-substituted imidazole - Monosaccharide - Imidolactam - Azole - Heteroaromatic compound - Tetrahydrofuran - Imidazole - 1,3-aminoalcohol - 1,2-aminoalcohol - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Organonitrogen compound - Organooxygen compound - Primary amine - Primary alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.

External Descriptors

Not available

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